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Single-cell RNA sequencing suggests new treatment options for diabetic kidney disease

A new study using a 1-million-cell atlas shows heterogeneity in kidney cell responses to diabetic kidney disease and treatments. Published […]

Lupus variants identified with whole-genome sequencing in Chinese patients

A new study has identified key rare variants in systemic lupus erythematosus (SLE) in a Chinese population for the first […]

Cancer Cell Metastases: Understanding the Process Using Insights from Single Cell Sequencing

This webinar will provide people working in cancer research and/or cancer therapy development with an understanding of how single cell […]

Exome sequencing in bipolar disorder identifies new risk gene

A study published in Nature Genetics from a consortium of researchers — the BipEx collaboration — is the largest whole-exome […]

Combining long and short read sequencing

Andrew Beggs, Mike Hubank and Matt Loose

Spatial and temporal RNA-sequencing

Sam Rodriques, Group Leader, Francis Crick Institute

Sequencing Data Released from a Liquid Biopsy Proficiency Study

Written by Charlotte Harrison, Science Writer  Liquid biopsy assays that detect circulating tumour (ct) DNA are safer and faster than […]

A History of Sequencing

Nucleic acid sequencing has become an integral part of modern biomedical research. The advances in sequencing technology, from its invention […]

Rapid Nanopore Sequencing Finds Disease-Causing Variants in Under 8 Hours

Written by Charlotte Harrison, science writer  Whole-genome sequencing can identify genetic variants that cause disease, but the time needed for […]

Impact of Next-Generation Sequencing for Lung Cancer Patients in East Asia

Written by Sharmin Begum, science writer  Next-Generation Sequencing (NGS) strategies were compared in patients with metastatic non-small cell lung cancer […]